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低剂量阿糖胞苷治疗急性髓系白血病的临床及血液学反应回顾

Review of clinical and haematological response to low-dose cytosine arabinoside in acute myeloid leukaemia.

作者信息

Shtalrid M, Lotem J, Sachs L, Berrebi A

出版信息

Eur J Haematol. 1987 Jan;38(1):3-11. doi: 10.1111/j.1600-0609.1987.tb01416.x.

DOI:10.1111/j.1600-0609.1987.tb01416.x
PMID:3472902
Abstract

15 patients with acute myeloid leukaemia (AML) were treated with low-dose cytosine arabinoside (LD ARA-C). 2 patients had complete remissions, which lasted for 8 and 3 months, and 5 patients had a partial remission. 46% of the patients thus responded to LD ARA-C. This included 1 responding patient who had not previously responded to therapy with 6-mercaptopurine, thioguanine, or vinblastine. The 2 patients with complete remission did not show LD ARA-C-induced hypoplasia of bone marrow, although 1 had hypoplastic AML before therapy. Leukaemic cells from 1 patient showed in vivo maturation from M1 to M3 after LD ARA-C treatment. The present results, together with the published data, indicate that: a. LD ARA-C treatment, although it may have some toxic effects, is an effective treatment for some patients with AML, especially those with hypoplastic AML; b. Response to LD ARA-C can be obtained after one or several courses of treatment; c. LD ARA-C-induced remissions are sometimes obtained even in patients who fail in more conventional treatments; d. LD ARA-C-induced remissions can be achieved without bone marrow hypoplasia, and induction of hypoplasia by itself does not always result in complete remission; e. LD ARA-C can induce in vivo maturation of leukaemic cells. It is suggested that induction of remission in AML patients by LD ARA-C may result from either differentiation of leukaemic blast cells, cytotoxicity to leukaemic blasts, or both mechanisms acting together.

摘要

15例急性髓系白血病(AML)患者接受了小剂量阿糖胞苷(LD ARA-C)治疗。2例患者完全缓解,缓解期分别持续8个月和3个月,5例患者部分缓解。因此,46%的患者对LD ARA-C有反应。这其中包括1例之前对6-巯基嘌呤、硫鸟嘌呤或长春花碱治疗无反应的有反应患者。2例完全缓解的患者未出现LD ARA-C诱导的骨髓发育不全,尽管其中1例在治疗前患有发育不全性AML。1例患者的白血病细胞在LD ARA-C治疗后显示出在体内从M1向M3的成熟。目前的结果与已发表的数据表明:a. LD ARA-C治疗虽然可能有一些毒性作用,但对一些AML患者是一种有效的治疗方法,尤其是那些患有发育不全性AML的患者;b. 在一个或几个疗程的治疗后可获得对LD ARA-C的反应;c. 即使在更传统治疗失败的患者中有时也能获得LD ARA-C诱导的缓解;d. LD ARA-C诱导的缓解可在无骨髓发育不全的情况下实现,而且发育不全本身并不总是导致完全缓解;e. LD ARA-C可诱导白血病细胞在体内成熟。提示LD ARA-C诱导AML患者缓解可能是由于白血病原始细胞的分化、对白血病原始细胞的细胞毒性或这两种机制共同作用的结果。

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1
Review of clinical and haematological response to low-dose cytosine arabinoside in acute myeloid leukaemia.低剂量阿糖胞苷治疗急性髓系白血病的临床及血液学反应回顾
Eur J Haematol. 1987 Jan;38(1):3-11. doi: 10.1111/j.1600-0609.1987.tb01416.x.
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Low-dose arabinosyl cytosine therapy of AML may be effective after failure of high or conventional doses.急性髓系白血病患者在高剂量或常规剂量治疗失败后,低剂量阿糖胞苷治疗可能有效。
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Low-dose cytosine arabinoside (LD-Ara C) treatment in dysmyelopoietic syndromes (DMPS) and acute myelogenous leukemia (AML).低剂量阿糖胞苷(LD-Ara C)治疗骨髓生成异常综合征(DMPS)和急性髓性白血病(AML)。
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[High dosage and intermediate dosage cytosine arabinoside in the treatment of secondary leukemias].[高剂量与中剂量阿糖胞苷治疗继发性白血病]
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引用本文的文献

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Differentiation of human leukaemic cell lines and fresh leukaemia cells by low dose Ara-C: monitoring by expression of c-myc and c-fos oncogenes.低剂量阿糖胞苷对人白血病细胞系和新鲜白血病细胞的分化作用:通过c-myc和c-fos癌基因表达进行监测
Med Oncol Tumor Pharmacother. 1988;5(2):91-7. doi: 10.1007/BF02985444.